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欧洲抗风湿病联盟(EULAR)药物治疗银屑病关节炎管理建议:2015 年更新。

European League Against Rheumatism (EULAR) recommendations for the management of psoriatic arthritis with pharmacological therapies: 2015 update.

机构信息

Sorbonne Universités, UPMC Univ Paris 06, Institut Pierre Louis d'Epidémiologie et de Santé Publique, GRC-UPMC 08 (EEMOIS), Paris, France Department of rheumatology, AP-HP, Pitié Salpêtrière Hospital, Paris, France.

Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria Second Department of Medicine, Hietzing Hospital, Vienna, Austria.

出版信息

Ann Rheum Dis. 2016 Mar;75(3):499-510. doi: 10.1136/annrheumdis-2015-208337. Epub 2015 Dec 7.

Abstract

BACKGROUND

Since the publication of the European League Against Rheumatism recommendations for the pharmacological treatment of psoriatic arthritis (PsA) in 2012, new evidence and new therapeutic agents have emerged. The objective was to update these recommendations.

METHODS

A systematic literature review was performed regarding pharmacological treatment in PsA. Subsequently, recommendations were formulated based on the evidence and the expert opinion of the 34 Task Force members. Levels of evidence and strengths of recommendations were allocated.

RESULTS

The updated recommendations comprise 5 overarching principles and 10 recommendations, covering pharmacological therapies for PsA from non-steroidal anti-inflammatory drugs (NSAIDs), to conventional synthetic (csDMARD) and biological (bDMARD) disease-modifying antirheumatic drugs, whatever their mode of action, taking articular and extra-articular manifestations of PsA into account, but focusing on musculoskeletal involvement. The overarching principles address the need for shared decision-making and treatment objectives. The recommendations address csDMARDs as an initial therapy after failure of NSAIDs and local therapy for active disease, followed, if necessary, by a bDMARD or a targeted synthetic DMARD (tsDMARD). The first bDMARD would usually be a tumour necrosis factor (TNF) inhibitor. bDMARDs targeting interleukin (IL)12/23 (ustekinumab) or IL-17 pathways (secukinumab) may be used in patients for whom TNF inhibitors are inappropriate and a tsDMARD such as a phosphodiesterase 4-inhibitor (apremilast) if bDMARDs are inappropriate. If the first bDMARD strategy fails, any other bDMARD or tsDMARD may be used.

CONCLUSIONS

These recommendations provide stakeholders with an updated consensus on the pharmacological treatment of PsA and strategies to reach optimal outcomes in PsA, based on a combination of evidence and expert opinion.

摘要

背景

自 2012 年欧洲抗风湿病联盟发布针对银屑病关节炎(PsA)的药物治疗建议以来,新的证据和新的治疗药物不断涌现。本研究旨在更新这些建议。

方法

系统检索了银屑病关节炎药物治疗的相关文献。随后,根据证据和 34 名工作组专家的意见制定了建议。分配了证据水平和推荐强度。

结果

更新后的建议包括 5 项总体原则和 10 项建议,涵盖了从非甾体抗炎药(NSAIDs)到传统合成(csDMARD)和生物(bDMARD)疾病修饰抗风湿药物的治疗方案,无论其作用机制如何,均考虑了银屑病关节炎的关节和关节外表现,但重点关注肌肉骨骼受累。总体原则涉及到需要共同决策和治疗目标。建议将 csDMARD 作为 NSAIDs 和局部治疗失败后的初始治疗方案,如有必要,再使用 bDMARD 或靶向合成 DMARD(tsDMARD)。通常首选肿瘤坏死因子(TNF)抑制剂作为一线 bDMARD。对于不适合使用 TNF 抑制剂的患者,可以选择靶向白细胞介素(IL)12/23(ustekinumab)或 IL-17 通路(secukinumab)的 bDMARD,或者不适合使用 bDMARD 时选用磷酸二酯酶 4 抑制剂(apremilast)等 tsDMARD。如果一线 bDMARD 策略失败,可以选择任何其他 bDMARD 或 tsDMARD。

结论

这些建议为利益相关者提供了基于证据和专家意见的共识,为银屑病关节炎的药物治疗和实现最佳治疗结局提供了更新的策略。

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